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Developed as a research compound to investigate selective GH axis stimulation, Ipamorelin is notable for its high selectivity for GH release with minimal impact on cortisol, prolactin or ACTH secretion compared to earlier generation GHRPs such as GHRP-2 and GHRP-6

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acnes led to an increased number of CD4 + lymphocytes and an enhanced phagocytosing activity and lymphokine-activated killing [84]

In cellular TRAF6-interacting receptors this position can be occupied by an aromatic or acidic amino acid 46

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